Canonical Allele Identifier: CA412941713

Gene: WDR45

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49074913C>T , CM000685.2:g.49074913C>T	GRCh38
NC_000023.10:g.48932572C>T , CM000685.1:g.48932572C>T	GRCh37
NC_000023.9:g.48819516C>T	NCBI36
NG_033004.1:g.30488G>A
NG_033004.2:g.31258G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376372.9:c.974-1G>A MANE Select	ENSP00000365551.3:n.974-1G>A
ENST00000322995.13:c.1007-1G>A	ENSP00000365543.5:n.1007-1G>A
ENST00000356463.7:c.977-1G>A	ENSP00000348848.3:n.977-1G>A
ENST00000367375.8:c.753-1G>A
ENST00000376358.4:c.521+451G>A	ENSP00000365536.3:n.521+451G>A
ENST00000376368.7:c.977-1G>A	ENSP00000365546.2:n.977-1G>A
ENST00000376372.8:c.974-1G>A	ENSP00000365551.3:n.974-1G>A
ENST00000396681.9:c.857-1G>A	ENSP00000379913.5:n.857-1G>A
ENST00000433252.7:n.852G>A
ENST00000465806.6:n.2131-1G>A
ENST00000473974.5:c.726-1G>A	ENSP00000417211.1:n.726-1G>A
ENST00000475977.2:c.324-1G>A	ENSP00000417754.2:n.324-1G>A
ENST00000485908.6:c.869-1G>A	ENSP00000419897.1:n.869-1G>A
ENST00000486337.6:c.162-13G>A
ENST00000634559.1:c.761-1G>A	ENSP00000488986.1:n.761-1G>A
ENST00000634838.1:c.932-1G>A	ENSP00000489268.1:n.932-1G>A
ENST00000634852.1:n.671-1G>A
ENST00000634944.1:c.974-1G>A	ENSP00000488972.1:n.974-1G>A
ENST00000635003.1:c.773-1G>A	ENSP00000489080.1:n.773-1G>A
NM_001029896.1:c.974-1G>A	NP_001025067.1:n.974-1G>A
NM_007075.3:c.977-1G>A	NP_009006.2:n.977-1G>A
NM_001029896.2:c.974-1G>A MANE Select	NP_001025067.1:n.974-1G>A
NM_007075.4:c.977-1G>A	NP_009006.2:n.977-1G>A